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Association between Polymorphisms in the IL-1β, TNFRSF11B, CASP1, and IL-6 Genes and Orthodontic-Induced External
Agata Ciurla1, Crystal Marruganti2, Tiziana Doldo3
1Dentist's Office ORTO-PUNKT, Mościckiego St. 72/1, 33-100 Tarnów, Poland.
Journal of Clinical Medicine
|September 28, 2021
Summary
Orthodontic-induced external apical root resorption (EARR) is a common complication. A specific gene variant in IL-1β significantly increases the risk of developing EARR during orthodontic treatment.
Area of Science:
- Genetics
- Orthodontics
- Dental Research
Background:
- Orthodontic-induced external apical root resorption (EARR) is a significant concern.
- The genetic basis of EARR remains largely undetermined.
- Identifying genetic predispositions can aid in risk assessment.
Purpose of the Study:
- To investigate the association between specific genetic polymorphisms (SNPs) in IL-1β, TNFRSF11B, CASP1, and IL-6 genes and EARR.
- To determine if these genetic variants influence the occurrence of EARR following orthodontic treatment.
Main Methods:
- Analysis of 101 patients' pre- and post-treatment radiographs (orthopantomograms and lateral cephalograms).
- Assessment of EARR presence using radiographic evaluation.
- Statistical analysis including Chi2 test and a binary logistic multi-level model to correlate SNPs with EARR.
Main Results:
- The overall prevalence of EARR was approximately 40%.
- A significant association was identified between EARR and a specific single nucleotide polymorphism (SNP) in the IL-1β gene.
- No significant association was found for SNPs in TNFRSF11B, CASP1, or IL-6 genes.
- The IL-1β gene SNP was found to increase the odds of developing EARR by approximately fourfold.
Conclusions:
- The IL-1β gene polymorphism is a potential predictive factor for EARR in orthodontic patients.
- Further research is necessary to explore other genetic variants and their role in EARR development.
- Developing predictive models for EARR is crucial due to the lack of accurate pre-treatment assessment methods.
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